FDAClass IIApril 17, 2019

Vyon DUALSTOP White Cap used for intravascular lines recall

Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular lines.

Why was Vyon DUALSTOP White Cap used for intravascular lines recalled?

DualStop Caps defect causing leaks in affected product

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot codes: 090718FD 250118FD 081117FD 130218FD 050418FD 020518FD

Product
Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular lines.
Recalling firm
Vygon U.S.A.
Quantity
107700
Distribution
US Nationwide distribution.
Recall date
April 17, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls